G41G (p.Gly41Gly) variant of AGXT (P21549)
G41G (p.Gly41Gly) in AGXT (P21549) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data, experimental measurements, published literature, and structural context.
G41G (p.Gly41Gly) variant details
- p.Gly41Gly
- rs769473982
- gnomAD 2-240868988-G-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0779
- CADD 0.12
- Most common in the South Asian population (allele frequency 3.5e-05)
- Structural context available
- AGXT complementation assay *1 B: score 0.492
- Literature evidence available